ENST00000479013.7:c.389G>T
|
ENSP00000417990.3:p.Gly130Val
|
|
ENST00000487418.8:c.479G>T
MANE Select
|
ENSP00000418397.3:p.Gly160Val
|
|
ENST00000610693.5:c.566G>T
|
ENSP00000479359.2:p.Gly189Val
|
|
ENST00000650656.1:c.398G>T
|
ENSP00000498731.1:p.Gly133Val
|
|
ENST00000651168.1:c.488G>T
|
ENSP00000499074.1:p.Gly163Val
|
|
ENST00000473112.6:c.238G>T
|
|
|
ENST00000479013.6:c.398G>T
|
ENSP00000417990.2:p.Gly133Val
|
|
ENST00000481262.6:c.85G>T
|
|
|
ENST00000484250.1:n.102G>T
|
|
|
ENST00000487418.6:c.488G>T
|
ENSP00000418397.2:p.Gly163Val
|
|
ENST00000558610.5:c.431G>T
|
ENSP00000453821.1:p.Gly144Val
|
|
ENST00000610693.4:c.575G>T
|
ENSP00000479359.1:p.Gly192Val
|
|
NM_001159508.1:c.398G>T
|
NP_001152980.1:p.Gly133Val
|
|
NM_002225.3:c.488G>T
|
NP_002216.2:p.Gly163Val
|
|
XM_005254350.2:c.488G>T
|
XP_005254407.1:p.Gly163Val
|
|
XM_005254356.2:c.488G>T
|
XP_005254413.1:p.Gly163Val
|
|
XM_006720491.2:c.431G>T
|
XP_006720554.1:p.Gly144Val
|
|
XM_006720492.2:c.488G>T
|
XP_006720555.1:p.Gly163Val
|
|
XM_006720493.2:c.488G>T
|
XP_006720556.1:p.Gly163Val
|
|
XM_006720494.2:c.488G>T
|
XP_006720557.1:p.Gly163Val
|
|
XM_006720495.2:c.488G>T
|
XP_006720558.1:p.Gly163Val
|
|
XM_011521523.1:c.488G>T
|
XP_011519825.1:p.Gly163Val
|
|
XM_011521524.1:c.488G>T
|
XP_011519826.1:p.Gly163Val
|
|
XR_243097.3:n.488G>T
|
|
|
XR_243098.2:n.488G>T
|
|
|
XR_429453.2:n.589G>T
|
|
|
NM_001159508.2:c.389G>T
|
NP_001152980.2:p.Gly130Val
|
|
NM_001354597.2:c.431G>T
|
NP_001341526.1:p.Gly144Val
|
|
NM_001354598.2:c.479G>T
|
NP_001341527.2:p.Gly160Val
|
|
NM_001354599.2:c.566G>T
|
NP_001341528.2:p.Gly189Val
|
|
NM_001354600.2:c.566G>T
|
NP_001341529.2:p.Gly189Val
|
|
NM_001354601.2:c.479G>T
|
NP_001341530.2:p.Gly160Val
|
|
NM_002225.4:c.479G>T
|
NP_002216.3:p.Gly160Val
|
|
NR_148925.1:n.889G>T
|
|
|
XM_006720495.3:c.488G>T
|
XP_006720558.1:p.Gly163Val
|
|
XM_017022149.1:c.575G>T
|
XP_016877638.1:p.Gly192Val
|
|
XM_017022150.1:c.575G>T
|
XP_016877639.1:p.Gly192Val
|
|
XM_017022153.1:c.575G>T
|
XP_016877642.1:p.Gly192Val
|
|
XM_017022154.2:c.518G>T
|
XP_016877643.1:p.Gly173Val
|
|
XM_017022155.2:c.575G>T
|
XP_016877644.1:p.Gly192Val
|
|
XM_017022157.1:c.575G>T
|
XP_016877646.1:p.Gly192Val
|
|
XM_017022158.2:c.575G>T
|
XP_016877647.1:p.Gly192Val
|
|
XR_001751263.1:n.838G>T
|
|
|
XR_001751264.1:n.879G>T
|
|
|
NM_001159508.3:c.389G>T
|
NP_001152980.2:p.Gly130Val
|
|
NM_001354597.3:c.431G>T
|
NP_001341526.1:p.Gly144Val
|
|
NM_001354598.3:c.479G>T
|
NP_001341527.2:p.Gly160Val
|
|
NM_001354599.3:c.566G>T
|
NP_001341528.2:p.Gly189Val
|
|
NM_001354600.3:c.566G>T
|
NP_001341529.2:p.Gly189Val
|
|
NM_001354601.3:c.479G>T
|
NP_001341530.2:p.Gly160Val
|
|
NM_002225.5:c.479G>T
MANE Select
|
NP_002216.3:p.Gly160Val
|
|
NR_148925.2:n.891G>T
|
|
|